4.8 Article

MicroRNA-9 Couples Brain Neurogenesis and Angiogenesis

期刊

CELL REPORTS
卷 20, 期 7, 页码 1533-1542

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2017.07.051

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资金

  1. NIH [NS062798, DK090065, MH099647, HG005058, F30MH106261, T32GM007365, MH099555-03]
  2. BrightFocus Foundation
  3. EMBO [ALTF 413-2012]
  4. National Science Foundation [DGE-1147470]
  5. Bio-X Stanford Interdisciplinary Graduate Fellowship
  6. Bio-X-Stanford Predoctoral Fellowship
  7. Packard Fellowship
  8. Stanford Dean's Postdoctoral Fellowship
  9. Child Health Research Institute [UL1-TR001085]
  10. NIMH BRAINS [R01MH107800]
  11. MQ Fellow Award
  12. Donald E. and Delia B. Baxter Foundation
  13. Kwan Foundation

向作者/读者索取更多资源

In the developing brain, neurons expressing VEGF-A and blood vessels grow in close apposition, but many of the molecular pathways regulating neuronal VEGF-A and neurovascular system development remain to be deciphered. Here, we show that miR-9 links neurogenesis and angiogenesis through the formation of neurons expressing VEGF-A. We found that miR-9 directly targets the transcription factors TLX and ONECUTs to regulate VEGF-A expression. miR-9 inhibition leads to increased TLX and ONECUT expression, resulting in VEGF-A overexpression. This untimely increase of neuronal VEGF-A signal leads to the thickening of blood vessels at the expense of the normal formation of the neurovascular network in the brain and retina. Thus, this conserved transcriptional cascade is critical for proper brain development in vertebrates. Because of this dual role on neural stem cell proliferation and angiogenesis, miR-9 and its downstream targets are promising factors for cellular regenerative therapy following stroke and for brain tumor treatment.

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